Anastasia Armimi, Afina Firdaus Syuaib, Katherine Vanya, M. Tan, D. Natalia, David Virya Chen, C. Ono, Y. Matsuura, A. Artarini, E. Giri-Rachman
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Optimal pseudo-lentivirus infection was analysed using fluorescent assay and luciferase assay. The optimal condition of pseudo-lentivirus infection was determined by the target cell type and the number of pseudo-lentiviruses used for neutralization test. SARS-CoV-2 pseudo-lentivirus was used to detect neutralizing antibodies from serum samples.RESULTS: The plasmid used for pseudo-lentivirus production was characterized and confirmed to have no mutations. Lipofectamine 2000 reagent generated pseudo-lentivirus with a higher ability to infect target cells, as indicated by a percentage green fluorescent protein (GFP) of 12.68%. Pseudo-lentivirus centrifuged obtained more stable results in luciferase expression. Optimal pseudo-lentivirus infection conditions were obtained using puromycin-selected HEK 293T-ACE2 cells as target cells. The number of pseudo-lentiviruses used in the neutralization assay system was multiplicity of infection (MOI) 0.075. 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引用次数: 0
摘要
背景:严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)感染人类下呼吸道并引起冠状病毒病-2019 (COVID-19)。中和抗体是一种适应性免疫系统反应,可以减少SARS-CoV-2感染。本研究旨在利用伪慢病毒建立SARS-CoV-2中和试验系统。方法:采用限制性内切法对制备伪慢病毒的质粒进行鉴定。测序证实了SARS-CoV-2刺突蛋白的编码基因。通过选择转染试剂和添加离心步骤,确定了伪慢病毒转染的最佳条件。采用荧光法和荧光素酶法分析最佳伪慢病毒感染。通过靶细胞类型和中和试验所用伪慢病毒的数量确定伪慢病毒感染的最佳条件。采用SARS-CoV-2伪慢病毒法检测血清样品中的中和抗体。结果:制备伪慢病毒的质粒经鉴定无突变。Lipofectamine 2000试剂产生的伪慢病毒感染靶细胞的能力更高,绿色荧光蛋白(GFP)百分比为12.68%。伪慢病毒离心后荧光素酶的表达更加稳定。以puromycin筛选的HEK 293T-ACE2细胞为靶细胞,获得最佳伪慢病毒感染条件。中和试验系统使用的伪慢病毒数为感染多重数(multiplicity of infection, MOI) 0.075。1:10稀释的血清A样品具有最高的中和抗体活性。结论:采用伪慢病毒的SARS-CoV-2中和试验系统可成功检测出人血清中的中和抗体,并降低了伪慢病毒的感染率。关键词:COVID-19,中和抗体,中和试验,伪慢病毒,SARS-COV-2
SARS-CoV-2 Neutralization Assay System using Pseudo-lentivirus
BACKGROUND: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infects humans' lower respiratory tracts and causes coronavirus disease-2019 (COVID-19). Neutralizing antibodies is one of the adaptive immune system responses that can reduce SARS-CoV-2 infection. This study aimed to develop a SARS-CoV-2 neutralization assay system using pseudo-lentivirus.METHODS: The plasmid used for pseudo-lentivirus production was characterized using restriction analysis. The gene encoding for SARS-CoV-2 spike protein was confirmed using sequencing. The transfection pseudo-lentivirus optimal condition was determined by choosing the transfection reagents and adding centrifugation step. Optimal pseudo-lentivirus infection was analysed using fluorescent assay and luciferase assay. The optimal condition of pseudo-lentivirus infection was determined by the target cell type and the number of pseudo-lentiviruses used for neutralization test. SARS-CoV-2 pseudo-lentivirus was used to detect neutralizing antibodies from serum samples.RESULTS: The plasmid used for pseudo-lentivirus production was characterized and confirmed to have no mutations. Lipofectamine 2000 reagent generated pseudo-lentivirus with a higher ability to infect target cells, as indicated by a percentage green fluorescent protein (GFP) of 12.68%. Pseudo-lentivirus centrifuged obtained more stable results in luciferase expression. Optimal pseudo-lentivirus infection conditions were obtained using puromycin-selected HEK 293T-ACE2 cells as target cells. The number of pseudo-lentiviruses used in the neutralization assay system was multiplicity of infection (MOI) 0.075. Serum A samples with a 1:10 dilution had the highest neutralizing antibody activity.CONCLUSION: This study shows that SARS-CoV-2 neutralization assay system using pseudo-lentivirus successfully detected neutralizing antibodies in human serum, which were indicated by a decrease in the percentage of pseudo-lentivirus infections.KEYWORDS: COVID-19, neutralizing antibody, neutralization assay, pseudo-lentivirus, SARS-COV-2